The following data is part of a premarket notification filed by Birtcher Corp. with the FDA for Bi-polar Forceps.
| Device ID | K854864 |
| 510k Number | K854864 |
| Device Name: | BI-POLAR FORCEPS |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | BIRTCHER CORP. 4501 N. ARDEN DR. P.O. BOX 4399 El Monte, CA 91731 |
| Contact | Donald L Emmons |
| Correspondent | Donald L Emmons BIRTCHER CORP. 4501 N. ARDEN DR. P.O. BOX 4399 El Monte, CA 91731 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-12-05 |
| Decision Date | 1985-12-24 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10653405014195 | K854864 | 000 |
| 10653405014188 | K854864 | 000 |
| 10653405014171 | K854864 | 000 |
| 10653405014164 | K854864 | 000 |
| 10653405014157 | K854864 | 000 |
| 10653405014140 | K854864 | 000 |
| 10653405014133 | K854864 | 000 |
| 10653405014126 | K854864 | 000 |
| 10653405014102 | K854864 | 000 |